CQV Engineer - Formulation & Component Prep

CQV Engineer - Formulation & Component Prep - Dublin, Ireland - 12 Month Contract

One of the top 10 best companies to work in Ireland is looking for a CQV Engineer for their large-scale new facility in Dublin. Is this you?

An exciting project there is lots of opportunity to learn new technology and develop current skills within a fast paced €1 billion project. This fantastic client offers the opportunity to work within a large-scale environment with cutting edge technology.

What you’ll do:

• Development and execution of CQV testing documentation for Equipment for the Sterile Drug product facility.
• Responsible for meeting key project deliverables for safety, CQV schedule and quality of project related documentation/electronic records for equipment assigned.
• Responsible for ensuring GMP equipment are tested in compliance with good manufacturing practices, company policies and EU & FDA regulations.
• Responsible for ensuring that all non GMP equipment, are tested in compliance with project related standards from a commissioning perspective.
• Deviation management associated with the assigned equipment and utilities.

What you’ll need:

• The ideal candidate should hold a minimum of a BS qualification (Degree) in a scientific, technical or engineering discipline
• Extensive experience within the pharmaceutical industrial ideally with familiarity with Sterile Drug Product filling line experience.
• Demonstratable capacity to effectively execute the CQV testing approach for assigned from initiation to completion.
• CQV project lifecycle experience from design through to C&Q and handover.
• Demonstrable experience of performing as part of diverse team of CQV professionals/ contractors to deliver on tasks safely, with quality focus, on time and within budget.

If this role is of interest, please apply now!

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